Rhododendron Ferrugineum L

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Volume 18(1), 123- 130, 2014
JOURNAL of Horticulture, Forestry and Biotechnology

www.journal-hfb.usab-tm.ro

Rhododendron ferrugineum L. and Rhododendron myrtifolium

Schott & Kotschy in habitats from Eastern Alps mountains and Carpathian Mountains

Căprar M.1,2, Cantor Maria2*, Szatmari P.1, Sicora C.1

1)Biological Research Center, Botanical Garden ,,Vasile Fati” Jibou, Parcului Street,no.14,455200 Jibou, Romania; 2)University of Agricultural Sciences and Veterinary Medicine Cluj-Napoca, Faculty of Horticulture, Mănăștur Street, no 3-5,4000472 Cluj-Napoca, Romania;

* Corresponding author. Email: [email protected]

Abstract

This paper presents results of research carried on two species Key words of Rhododendron in habitats from different regions of Central and Eastern

Europe (Rhododendron ferrugineum and Rhododendron myrtifolium). It rhododendrons

species, presents the ecological requirements of each habitat, their spread, main plant habitats, plant communities, association and floristic composition based on the dominance of probative Carpathian Mountains, Alps species. A correlation is made between habitats from different classifications, Mountains but with the same features, mentioning EUNIS codes, Emerald, Natura 2000, Palaearctic Habitats and the European forest types. This paper presents information on the spread of two types of habitats containing Rhododendronfrom Europe, the environmental conditions in which they live and the accompanying species involved, more or less, in the composition of habitats. It describes the types of vegetation in the Alps (Austria) and the Carpathian Mountains (Romania). Vegetation was observed following the research in the field.

Knowledge of the habitats in which
Rhododendron species live becomes an important objective in order to protect these species that in most European countries are rare or endangered. The rhododendron habitats host a series of species that are rare and scientifically interesting, from witness of ice ages to survivors of Tertiary or unique endemic species. Conservation of these habitats will help perpetuate the species and better understand the functioning of ecosystems. of Australia, with over 200 species only in the island of New Guinea [2].
Rhododendron species vary in shape and height from miniature plants, repentis that forme pads under the action of external factors, as far as 30 m trees in mountain forests. Many species grow at high altitudes, over 900 m, some on rocks, some are epiphytic on tree branches. They occupy a wide variety of ecosystems, tropical mountain forests and alpine meadows at 4000 m altitude [19].

  • The genus Rhododendron L. (in ancient Greek
  • Flowers may be solitary or in up to 24

- "rhodon" the rose, and "dendron" meaning tree) [11] belongs to the family Ericaceae, a highly complex genre, totaling over 1000 species worldwide. According to Heywood there are around 700 species only in the region covering China, Tibet, Nepal, Assam (Northeast India) and Myanmar [12]. Woody species, some of which are evergreen, others deciduous, meet along the entire northern hemisphere. Most are found in temperate and cold regions with a high concentration of species in western China, the Himalayas and northeastern Myanmar (Burma) [16]. Due to unfavorable conditions some of them have adapted by losing leaves in winter most frequent seem in North America, China, Japan and Europe. Tropical rhododendrons, generically called "Vireya" [16], grow at high altitudes in Southeast Asia (Indochina), up to the south in Indonesia, Philippines and northern parts racemes, the species has a wide range of colors, maybe one of the richest in the plant world, some parts of the flower can be poisonous. Flowering period can begin in early spring in different species until late summer, some even in fall, and the tropical ones throughout the year. The fruit is usually a woody capsule, rarely soft, with many seeds, sometimes wearing wings and appendages to facilitate air transport [16]. All species of Rhododendron form mycorrhizae with various species of fungi in a wide variety of habitats [21].
The Ericaceae family has been divided into several subfamilies, Rhododendron genus entering Rhodoreae tribe from Ericoideae subfamily, the

  • subfamily
  • which
  • includes
  • the

Ericagenus,
Bruckenthalia and Calluna, grown under similar

conditions. The genus has been subdivided into several subgenera where azaleas, formerly classified separately in Azaleagenus, are now also classified in the

123

Rhododendron genus, but with a clear status, the 5 anthers from the flower making them easily distinguishable from true rhododendrons [29]. are found in the Apuan Alps in Italy (Tuscany), which is considered a relic of the cold climate [3].

New genetic studies have shown that Ledum

2. Rhododendron myrtifolium Schott & Kotschy

species, until recently treated separately, must be placed in the Rhododendron genus, thereby a new subsection was added. Because most names from Ledum species have been used in other species of the Rhododendron genus, new names were given, for example the species Ledum palustre became

Rhododendron tomentosum and Ledum decumbens became Rhododendron subarcticum wich most often is

treated as a subspecies of Ledum palustre. Instead

Ledum groenlandicum kept the name Rhododendron groenlandicum[10,14].

  • Small
  • shrub
  • (10-50
  • cm),
  • that

hascrenate,obtuse, evergreen leaves, with pink flowers and pubescent pedicels, toxic, grows especially on shady slopes and rockery [20, 5]. A Carpatho-Balkan species, oligotrophic, mesophilic, moderate to strong acidophile, calcifuge [17, 18].
It is widespread in the Carpathian Mountains
(Eastern and Southern Carpathians - Romania, western Ukraine, but missing from the Carpathians in Slovakia), in the Balkan Mountains and Rila (Bulgaria) and in northern Macedonia, Serbia, Kosovo, Albania [20, 5, 13, 27]. The species is protected in Ukraine (where populations are declining), Bulgaria and Romania [4, 18].

1. Rhododendron ferrugineum L.

Rhododendron ferrugineum is a small shrub

(30-120 cm, maximum 1.8 m) evergreen with dark green elliptical leaves, densely covered underneath with reddish-brown (rust) scales, hence the scientific name. The flowers are deep pink to purple [16, 1]. The leaves are toxic, after consumption can cause damage to the digestive, circulatory, nervous and respiratory system [29].

Material and Methods

The methods used in the study of plant communities from mountain areas are based on observation, description, collecting material for genetic and structural laboratory tests. Analysis of floristic composition and the phytocoenosis structure was made through field and laboratory activities. In order to determine the species, the following papers were used: Flora Europaea, vol. I – IV (1964 – 1980), Flora Alpina – Aeschimann 2004, Flora ilustrata a Romaniei – Ciocarlan, 2009. Research methods were based on criteria developed by Braun – Blanquetusing the surveys conducted in the summer months in both the Alps and the Carpathians (Fig.1, 2).
A Southern European species, widespread in the high mountain (subalpine) zone of the Alps

  • (Southern
  • Germany,
  • Austria,
  • Liechtenstein,

Switzerland, southeastern France, northern Italy, northwestern Slovenia), Pyrenees (southern France, northern Spain, Andorra), Jura Mountains (eastern France, north-western Switzerland and west Germany), Northern Apennines (central Italy) and the Dinaric Mountains (Slovenia, northern Croatia, Serbia, Kosovo, Macedonia, Albania) [1, 26]. It was introduced in the Czech Bohemian Massif [28]. It is protected in Austria, Italy, Slovenia, Croatia and Serbia [28].

Rhododendrons habitats researched in this paper

Habitat description was made for each species of Rhododendron depending on the geographic area it occupies. Habitats addressed in the paper are filled with official denomination of the habitats found under different names but with the same species and ecological requirements, from many scientific studies published over the years, greatly helping identification and correlation between them. The paper also presents phytocenologic surveys on plants identified in each habitat.
It forms large thickets in mountainous upper floors, in open places, steep slopes or rare forest [20].
Cold climate element, refugee in the upper floors of the mountains, rarely may occur under 1600 m. One such place is the resort Schrottkogel, southwest of Klagenfurt in Carinthia (Austria), at just 700 m altitude, it is considered a glacial relict [8]. Also it was observed that it can survive in the Sphagnum bogsin the southern Alps, Tyrol region, Italy [9] or in the Julian Alps in Slovenia together with Pinus mugo[15]. In the northern Apennines Mountains of Italy,

Rhododendron ferrugineum populations are considered relics. Rhododendron ferrugineum is found only on a

few massive such as Cima Belfiore (1810 m), Mount Prado (2053 m), Mount Libro Aperto (1937 m), where these populations grow on the northern slopes between 1750-1937 m altitude. The conservation of these populations is due to heavy rainfall and acid soil [7].

Other small populations of Rhododendron ferrugineum

Results and Discussions

Alpine and subalpine scrubland with Rhododendron

ferrugineum

Biotope: Rhododendron ferrugineum form large under

wood in rocky and grassy places, especially in the subalpine level of the Alps, along with other short or tall evergreen, alpine bushes such as Pinus mugo, resistant to severe frost, between 1600-2500 m altitudes. The

124

main spread is influenced by soil specifics, so it will be found only on acid soils with siliceous rock substrate (bedrock, granite, etc.), poor in nutrients, clayey or peaty and rich with moist humus. Plants can survive on clay soils if constant wet air masses are in the area. On the northern slopes of the French Alps was observed

that the populations of Rhododendron ferrugineum

abound especially because there is reduced grazing in the area. Rhododendrons population has declined in all Central Europe massifs where intensive grazing is practiced.

Plant associations: Rhododendretum ferruginei Rübel

1911

Structure and floristic composition: This

habitat is well represented in the Austrian Alps where

Rhododendron ferrugineum are found on podzolic acid

soils in alpine and subalpine areas often with dwarf pines and other crawling shrubs with a compact layer of moss.
Dominant species and characteristic species:

Rhododendron ferrugineum, Vaccinium myrtillus, Pinus mugo, Avenella flexuosa, Diphasiastrum alpinum, Huperzia selago, Lonicera caerulea, Pyrola minor. Other important species: Juniperus communis ssp. nana, Dryas octopetala, Polygonum bistorta, Veratrum album, Clematis alpina, Empetrum hermaphroditum, Loiseleuria procumbens, Vaccinium uliginosum ssp. pubescens.

Synonyms used for this habitat

- 4060 Alpine and Boreal heaths (EU Habitats
Directive Annex 1)
(Acidocline alpenrose heaths (Rhododendro-

Vaccinion Schnyder 1930))

- 4060 Landes subalpines acidiphiles hautes à
Rhododendron ferrugineux (CORINE)
- F2.2 Evergreen alpine and subalpine heath and scrub (EUNIS)
- 31.4 Alpine and boreal heaths (Palearctic
Habitats)
In this habitat we find many endemic plants

for the Alps like:Delphinium elatum subsp. austriacum, Pulsatilla alpina subsp. schneebergensis, Pulsatilla alpina subsp. austriaca, Cerastium pedunculatum, Cerastium charantiacum subsp. charintiacum. Other

species from the same habitat are: Vaccinium myrtillus,

Calamagrostis villosa, Valeriana celtica ssp. norica, Cystopteris montana, Vaccinium vitis-idaea, Huperzia selago, Dryopteris expansa, Solidago virgaurea ssp. minuta, Empetrum hermaphroditum, Homogyne alpina, Vaccinium gaultherioides, Oxalis acetosella.

- F2.2 Alpide acidocline [Rhododendron] heaths (EUNIS)
- 31.42 Alpide acidocline alpenrose heaths
(Palearctic Habitats)

  • -
  • F2.3 Subalpine and oroboreal bush

communities (EUNIS)

  • -
  • 31.6 Subalpine and arboreal bush

communities (Palearctic Habitats)

Fig. 1. Locations where observations were made in the Alps for Rh. Ferrugineum (red dots)

125

Fig. 2. Rhododendron ferrugineum in the Alps (Klausen Pass – 1952 m altitude - Austria)
Table 1

Rhododendron ferrugineum field surveys in the Alps (Austria)

Field survey number Altitude Exposition Herb cover (%) Sample area (m2)

Rhododendron ferrugineum Vaccinium myrtillus Pinus mugo

1
1952 N

80 25
4

2
2078 NE

90 25
5

3
2101 N

70 25
4
3+
3-
2+

Larix decidua

  • -
  • -
  • +

Gentiana burseri Vaccinium gaultherioides Juniperus sibirica Juncus trifidus

-321
+312
+212

Luzula sieberi

  • +
  • -
  • +

Blechnum spicant Calluna vulgaris Avenella flexuosa Homogyne alpina Lonicera nigra

+-1+
++++
--2+

  • -
  • +
  • -

Huperzia selago Melampyrum sylvaticum Pyrola minor

++-
-++
---

Nardus stricta

  • +
  • 1
  • +

126

Gentiana punctata Anthoxanthum alpinum Geum montanum Festuca varia Orthilia secunda Arctostaphylos uva-ursi Solidago virgaurea subsp. minuta Leontodon helveticus Luzula alpinopilosa Arnica montana

-++++-+-+++-++++-
++-+--+-+--+-++++1+
--++-+++++-+--+--

Pinus cembra Agrostis rupestris Deschampsia cespitosa Empetrum nigrum subsp. hermaphroditum Poa chaixii Calamagrostis villosa Cystopteris montana Vaccinium vitis-idaea Campanula alpina

+-
+-

  • Alpine and subalpine scrubland with Rhododendron
  • Synonyms used for this habitat

myrtifolium

- 4060 Alpine and Boreal heaths (EU Habitats

  • Directive Annex 1)
  • Biotope: In Romania this habitat is frequent

on large areas in subalpine and alpine floors, especially in the juniper zone, between 1800 - 2200 (2300) m altitude with heavy rainfall (Fig. 3).
- 31.4 Alpine and Boreal heaths (CORINE)

- F2.224 Carpathian Rhododendron kotschyi

heaths (Emerald)

F2.225 Balkan Rhododendron kotschyi

heaths (Emerald)

- F2.2 Carpathian [Rhododendron kotschyi]

heaths (EUNIS)

- F2.2 Balkan [Rhododendron kotschyi] heaths

(EUNIS)
These habitats are installed on slopes and

-

ridges with northern and northeastern exposition, with medium or large inclinations. The substrate consists of siliceous rocks, rarely limestone. Soils are shallow, skeletal lithosols, sometimes on screen, with strong acid to acid reaction (pH 4.7 to 5.4). It is a habitat that requires protection, especially in Bucegi Mountains being subjected to numerous human activities with negative impact especially overgrazing, destruction of shrub vegetation to increase grassland surface in these

areas. Also Rhododendron myrtifolium is quite

sensitive to late and heavy frosts, being stronger developed only in areas with permanent snow and full coverage. The habitat has a high conservation value, sheltering many rare, vulnerable and endemic plants

such as: Campanula serrata, Salix retusa, Viola alpina, Armeria alpina.

  • -
  • 31.424 Carpathian Kotschy's alpenrose

heaths (Palearctic Habitats)
- 31.425 Rhodopide and Balkan Kotschy's alpenrose heaths (Palearctic Habitats)

  • -
  • R3104 Rhododendron scrubland southeast

(Rhododendron myrtifolium) with

Carpathian

blueberries (Vaccinium myrtillus) [6]

Plant associations Rhododendro myrtifolii

Vaccinietum

  • (Borza
  • 1959)
  • Boscaiu
  • 1971.

127

Fig. 3. Locations where observations were made in the Carpathian Mountains for Rh. myrtifolium

scoparium, Hylocomyum splendens, Polytrichum juniperinum. Other important species: Bruckenthalia spiculifolia, Pinus mugo, Juniperus sibirica, Campanula abietina, Campanula serrata, Pinus cembra, Carex atrata, Avenula versicolor, Picea abies, Luzula sylvatica, Soldanella hungarica ssp.major, Calamagrostis villosa, Lonicera caerulea, Oxalis acetosella, Deschampsia flexuosa, Melampyrum sylvaticum, Huperzia selago, Lycopodium annotinum, Potentilla aurea ssp. chrysocraspeda.Rhododendron

myrtifolium under wood is widespread in Bucegi Mountains where they have an ecological role in

Structure and floristic composition:

Generally the species involved are of alpine, circumpolar and boreal origin, most of them acidophilus. Phytocoenosis is primary, but may extend secondary on degraded soils, deforested spruce and juniper forest trees. Dominant species and

characteristic: Rhododendron myrtifolium (Rh. kotschy) (Fig. 4), Vaccinium myrtillus, Vaccinium vitis- idaea,Vaccinium gaultherioides, Saxifraga paniculata, Campanula kladniana. They achieve coverage of 80-

100%. Grasses layer is dominated by: Nardus stricta,

Anthoxanthum odoratum, Luzula luzuloides, Potentilla ternata, Homogyne alpina, Loiseleuria procumbens, Geum montanum and a series of moss: Dicranum

  • stabilizing
  • coast
  • and
  • screens.

Fig. 4. Rhododendron myrtifolium in Bucegi Mountains (Furnica Mountain – 2028 m altitude)

128

Table 2

Rhododendron myrtifoliumsurvey in the Carpathian Mountains (Retezat)

Survey number Altitude Exposition Herb cover (%)

1
1990 NE

90 25
4321+-

2
2025 N

70 25
532+++++-+-++-+---+-------

3
2040 N

60 25
4211+++++----+-----+-++-+-+---+-+-
Sample area (m2)

Rhododendron myrtifolium Vaccinium gaultherioides Vaccinium myrtillus Vaccinium vitis-idaea Campanula alpina Saxifraga paniculata Campanula kladniana Nardus stricta Anthoxanthum odoratum Potentilla ternata Bruckenthalia spiculifolia Primula minima Homogyne alpina Festuca supina Luzula luzuloides Loiseleuria procumbens Geum montanum Pinus cembra Campanula serrata Luzula sylvatica

11++++++++++-+++-+-

Calamagrostis villosa Avenula versicolor Lonicera caerulea Melampyrum sylvaticum Carex atrata Soldanella hungarica subsp. major Deschampsia flexuosa Huperzia selago

+

  • -
  • +

+---
++++++-+-+-

Picea abies Lycopodium annotinum Potentilla aurea subsp. chrysocraspeda Dianthus gelidus Juncus trifidus Oxyria dygina Thymus pulcherrimus Viola alpina Senecio carpaticus Oxytropis halleri

-+++--+
++-+

From observations made on the field can conclude that these habitats have a fragile structure and can be easily affected by human activities such as excessive grazing and tourist activities.

Conclusions

  • Rhododendron
  • ferrugineum

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    Pollen Morphology and Its Systematic Significance in the Ericaceae

    Title Pollen Morphology and Its Systematic Significance in the Ericaceae Author(s) Sawara, A.K.M. Golam Citation 北海道大学. 博士(農学) 甲第8187号 Issue Date 2007-03-23 DOI 10.14943/doctoral.k8187 Doc URL http://hdl.handle.net/2115/46925 Type theses (doctoral) File Information sarwar.pdf Instructions for use Hokkaido University Collection of Scholarly and Academic Papers : HUSCAP Pollen Morphology and Its Systematic Significance in the Ericaceae (ツツジ科植物の花粉形態とその体系学的意義) A dissertation submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy By Sarwar, A.K.M. Golam Division of Bioresources and Product Science Graduate School of Agriculture Hokkaido University Sapporo, Japan March, 2007 Contents Abstract iv Chapter 1: GENERAL INTRODUCTION 1 Chapter 2: MATERIALS AND METHODS 10 Chapter 3: POLLEN MORPHOLOGY AND ITS SYSTEMATIC SIGNIFICANCE 20 GENERAL POLLEN MORPHOLOGY OF THE ERICACEAE 20 3-1 SUBFAMILY ENKIANTHOIDEAE 24 Introduction 24 Results 25 Discussion 30 3-2 SUBFAMILY ARBUTOIDEAE 44 Introduction 44 Results 45 Discussion 51 3-3 SUBFAMILY ERICOIDEAE 60 Introduction 60 Results 61 Discussion 81 3-4 SUBFAMILY CASSIOPOIDEAE 106 Introduction 106 Results 107 Discussion 110 ii 3-5 SUBFAMILY HARRIMANELLOIDEAE 112 Introduction 112 Results 113 Discussion 113 3-6 SUBFAMILY VACCINIOIDEAE 118 Introduction 118 Results 119 Discussion 160 Chapter 4: GENERAL DISCUSSION 203 Acknowledgements 252 Summary 254 References 259 Appendix I: Different classification systems of Ericaceae 281 Appendix II: Specimens examined 287 iii Abstract A detailed description of the range of pollen morphological variation within the family Ericaceae sensu Kron et al. (2002a) has been presented. For this palynological investigation, 275 taxa of 270 species representing 57 genera and 6 subfamilies were studied with light (LM) and scanning electron microscopy (SEM), and 31 species with transmission electron microscopy (TEM).
  • Molecular Phylogenetics and Patterns of Floral Evolution in the Ericales

    Molecular Phylogenetics and Patterns of Floral Evolution in the Ericales

    Int. J. Plant Sci. 166(2):265–288. 2005. Ó 2005 by The University of Chicago. All rights reserved. 1058-5893/2005/16602-0009$15.00 MOLECULAR PHYLOGENETICS AND PATTERNS OF FLORAL EVOLUTION IN THE ERICALES Ju¨rg Scho¨nenberger,1,* Arne A. Anderberg,y and Kenneth J. Sytsma* *Department of Botany, University of Wisconsin, Madison, Wisconsin 53706-1831, U.S.A.; and yDepartment of Phanerogamic Botany, Swedish Museum of Natural History, SE-104 05 Stockholm, Sweden The diverse and species-rich order Ericales has found considerable interest among systematists in recent years. Molecular phylogenetic studies not only have convincingly demonstrated the monophyly of the order, comprising 23 families formerly placed in three different subclasses (Asteridae, Dilleniidae, and Rosidae), but have also resolved Ericales as sister to euasterids. Most ericalean families are well circumscribed and have been or are currently subject to intrafamilial phylogenetic studies. In spite of all the attention that Ericales have received recently, there remains a major challenge, the still largely unresolved deeper nodes in the ericalean phylogeny. This study aims to improve our current knowledge of the interfamilial relationships by expanding on gene and taxon sampling and to evaluate the evolution of important floral characters in light of the resulting phylogeny. We add a nuclear region (26s rDNA) to already published data sets (nuclear: 18s rDNA; mitochondrial: atp1, matR; chloroplast: atpB, ndhF, rbcL, matK, the rps16 intron, the trnT-trnF spacer, and the trnV-atpE spacer), for a total of 11 molecular markers that include nearly 20 kb of sequences. Our analyses, applying both maximum parsimony and Bayesian inference, resolve some of the deeper nodes in the phylogeny.
  • Could Bryophagous Beetles (Coleoptera: Byrrhidae) Help Us Understand Bryophyte Taxonomy? Preferences Within the Hypnum Cupressiforme Hedw

    plants Article Could Bryophagous Beetles (Coleoptera: Byrrhidae) Help Us Understand Bryophyte Taxonomy? Preferences within the Hypnum cupressiforme Hedw. Species Complex Petr Pyszko 1,*, Michaela Drgová 1, Stanislav Ožana 1, OndˇrejDor ˇnák 1, David Rožek 2, Daniel Lee Cˇ íp 2, VítˇezslavPlášek 1 and Pavel Drozd 1 1 Department of Biology and Ecology/Institute of Environmental Technologies, Faculty of Science, University of Ostrava, Chittussiho 10, 710 00 Ostrava, Czech Republic; [email protected] (M.D.); [email protected] (S.O.); [email protected] (O.D.); [email protected] (V.P.); [email protected] (P.D.) 2 Heyrovsky High School of Chemistry, Stˇredoškolská 2854/1, 700 30 Ostrava, Czech Republic; [email protected] (D.R.); [email protected] (D.L.C.)ˇ * Correspondence: [email protected]; Tel.: +420-608-546-079 Abstract: Intrataxonomic differences in terms of angiosperm suitability for herbivorous insects stem from variables such as plant structure, palatability, and chemistry. It has not yet been elucidated whether these differences also occur in terms of the bryophyte’s suitability to bryophages. Hypnum cupressiforme Hedw. is a morphologically variable moss species frequently inhabited or fed by insects. In this investigation, we offered five morphotypes of H. cupressiforme to two bryophagous species of Citation: Pyszko, P.; Drgová, M.; Byrrhidae (Coleoptera) to reveal whether the intrataxonomic variability affects beetles’ preferences. Ožana, S.; Dorˇnák,O.; Rožek, D.; Lee The morphotypes were offered with preserved and removed spatial structures. There were no Cíp,ˇ D.; Plášek, V.; Drozd, P. Could significant differences in morphotype preferences when spatial structures were preserved, although Bryophagous Beetles (Coleoptera: flat usual turgid Byrrhidae) Help Us Understand during the daytime, the beetles moved from the morphotype to the and morphotypes.
  • Appendix S1 Species Richness of Lepidoptera and Auchenorrhyncha on Native Trees and Shrubs in Germany and the Range Size of the Host Plants (Number of Occupied Grids)

    Appendix S1 Species Richness of Lepidoptera and Auchenorrhyncha on Native Trees and Shrubs in Germany and the Range Size of the Host Plants (Number of Occupied Grids)

    Appendix S1 Species richness of Lepidoptera and Auchenorrhyncha on native trees and shrubs in Germany and the range size of the host plants (number of occupied grids). Range size was extracted from grid maps (10 min longitude x 6 min latitude, ≈ 130 km 2). Note that in the compilation only host records that reported the host species were considered; those that reported only the genus were not. Host plant species Family Order Lep. Auch. Range size Abies alba Pinaceae Coniferales 15 0 558 Acer campestre Aceraceae Sapindales 25 12 1917 Acer monspessulanum Aceraceae Sapindales 0 2 43 Acer opalus Aceraceae Sapindales 0 0 - Acer platanoides Aceraceae Sapindales 12 7 2083 Acer pseudoplatanus Aceraceae Sapindales 29 13 2152 Alnus alnobetula Betulaceae Fagales 0 2 54 Alnus glutinosa Betulaceae Fagales 39 19 2168 Alnus incana Betulaceae Fagales 9 11 849 Amelanchier ovalis Rosaceae Rosales 1 0 190 Berberis vulgaris Berberidaceae Ranunculales 6 0 1070 Betula humilis Betulaceae Fagales 2 0 54 Betula nana Betulaceae Fagales 0 0 19 Betula pendula Betulaceae Fagales 76 28 2171 Betula pubescens Betulaceae Fagales 22 11 1745 Betula x aurata Betulaceae Fagales 0 0 30 Buxus sempervirens Buxaceae Euphorbiales 0 2 35 Calluna vulgaris Ericaceae Ericales 38 6 2051 Carpinus betulus Corylaceae Fagales 45 11 2124 Chamaecytisus ratisbonensis Fabaceae Fabales 0 0 57 Chamaecytisus supinus Fabaceae Fabales 0 0 29 Clematis alpina Ranunculaceae Ranunculales 2 0 12 Clematis vitalba Ranunculaceae Ranunculales 23 0 1556 Cornus mas Cornaceae Cornales 1 1 114 Cornus sanguinea
  • Disparity in Sr and Cs Uptake in Alpine Plants

    Disparity in Sr and Cs Uptake in Alpine Plants

    View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by RERO DOC Digital Library Plant Soil (2012) 355:29–39 DOI 10.1007/s11104-011-1110-6 REGULAR ARTICLE Disparity in 90Sr and 137Cs uptake in Alpine plants: phylogenetic effect and Ca and K availability Thomas Guillaume & Fabienne Chawla & Philipp Steinmann & Jean-Michel Gobat & Pascal Froidevaux Received: 8 September 2011 /Accepted: 15 December 2011 /Published online: 4 February 2012 # Springer Science+Business Media B.V. 2012 Abstract on 6 undisturbed and geochemically different soils in Background and aims Uptake of 90Sr and 137Cs in the Alpine valley of Piora, Switzerland. plants varies widely between soil types and between Results Results show that a strong correlation exists plant species. It is now recognized that the radionu- between the log TF and the log of exchangeable Ca or clide uptake in plants is more influenced by site- K of the soils. specific and plant-specific parameters rather than the Conclusions Cs uptake by Phleum rhaeticum (Poales) bulk radionuclide concentration in soil. We hypothe- and Alchemilla xanthochlora (Rosales) is more sensi- sized that the stress which Alpine plants experience tive to the amount of exchangeable K in the soil than because of the short growing season may enhance the the corresponding uptake by other orders. Moreover, phylogenetic effect on the 137Cs and 90Sr transfer the 90Sr results indicate a phylogenetic effect between factors as well as the dependency of the uptake by Non-Eudicot and Eudicots: the order Poales (Phleum plant to the concentrations of exchangeable Ca and K rhaeticum) concentrating much less 90Sr than Eudicots of soils.
  • A Taxonomic Review of the Yellow-Flowered Species Of

    A Taxonomic Review of the Yellow-Flowered Species Of

    i Thesis submitted in partial fulfillment of the M.Sc. in the Biodiversity and Taxonomy of Plants: A taxonomic review of the yellow-flowered species of Rhododendron L. subsection Maddenia (Hutch) Sleumer by Flora Donald 20th August 2012 ii DECLARATION I declare that all of the original work presented in this study is my own. All external sources of information have been acknowledged fully by citation of the authors in the text and full publication details listed in the reference section. All illustrations included in this study that were not designed by F. Donald have been acknowledged with regard to the original place of publication. All photographs have been supplied by F. Donald. Flora Donald 20th August 2012 Frontispiece: R. burmanicum x R. valentinianum by Stones, M. In: Taylor, G. ed., 1969. Curtis’s Botanical Magazine, 177(2), p.546. iii ABSTRACT Rhododendron L. subsection Maddenia (Hutch) Sleumer primarily contains lepidote species with white flowers but nine (including one potentially new species) are yellow-flowered. The aim of this study was determine if these species were taxonomically distinct and formed a monophyletic subgroup within the subsection. These aims were investigated by the morphological characterisation of 64 herbarium specimens, including scanning electron microscopy of 15 specimens, and geo-referencing specimens to visualise the biogeographic relationships of the species. Twenty-six sequences of the matK chloroplast region representing 17 taxa were generated using the Qiagen method. This data matrix was expanded by including Rhododendron sequences from GenBank and analysed using maximum parsimony and maximum likelihood phylogenetic techniques. These analyses found all eight yellow-flowered species investigated to be justifiable and a taxonomic account was written to present these findings.